FDA.reportPublic FDA data

Duploject Easy Prep

Primary DI
50085412095634
Brand
Duploject Easy Prep
Company
BAXTER INTERNATIONAL INC.
Model
1501252
Catalog number
1501252
Device description
Fibrin Sealant Preparation and Application System for the preparation and application of Tisseel Two-component Fibrin Sealant (10 mL Kit)
Published
2016-09-24
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
FMFSyringe, piston

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FMFSyringe, PistonGeneral Hospital2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K020666000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K020666000DUPLOJECT EASY-PREP SYSTEM 1ML, 2ML, 5MLBaxter Healthcare Corp2002-06-24FMF

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
50085412095634PackageGS16In Commercial Distribution
00085412095639PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
5008541209563450085412095634
00085412095639000854120956390854120956390085412095639

GMDN Terms#

Term, Definition table
TermDefinition
Open-surgery adhesive/sealant applicator, dual-channelA sterile dual-channel delivery device designed to enable a surgeon to apply with precision a two-component medication or adhesive/sealant to a surgical site during open surgery (e.g., arterial anastomosis, colonic anastomosis, and vascular graft reconstruction). The device, also known as a surgical sealant dispenser (SSD), is typically made of flexible metal or synthetic material, and has a connector at one end to attach a compatible dispensing device (e.g., a dual-component syringe). This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Total Volume10Milliliter

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)933-0303Medinfo_medproducts@baxter.com

Regulatory Flags#

DUNS number
005146311
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
true
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00085412001814Baxter2C56452C56452016-09-24
00085412002996Baxter2C92212C92212016-09-24
00085412003900Baxter2C62262C62262016-09-24
00085412003917Baxter2C62272C62272016-09-24
00085412004846MICRO-VOLUME2N33502N33502016-09-24
00085412013718Baxter1C83631C83632016-09-24
00085412020716Baxter1C81891C81892016-09-24
00085412021096Baxter1C82731C82732016-09-24
00085412032085Baxter1C86571C86572016-09-24
00085412079714BaxterACT5612ACT56122016-09-24
00085412079721BaxterACT6227ACT62272016-09-24
00085412002286INTERLINK/CONTINU-FLO2C65722C65722016-09-24
00085412002347INTERLINK2C66072C66072016-09-24
00085412002361INTERLINK2C66312C66312016-09-24
00085412003955INTERLINK2C66062C66062016-09-24
00085412004921INTERLINK2N33762N33762016-09-24
00085412013619INTERLINK1C83331C83332016-09-24
00085412014135INTERLINK1C84541C84542016-09-24
00085412017853INTERLINK/CONTINU-FLO3C00913C00912016-09-24
00085412051314CLEARLINK2N83772N83772016-09-24

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